FoodMay 11, 2022
Bakkavor Foods USA WHOLE FOODS MARKET red lentil dal NET WT recall — FDA F-1043-2022
Possible Listeria monocytogenes in product
Class IFDA: TerminatedBakkavor Foods USA Inc.
Latest records
Latest recalls — page 734
The newest recall records with useful source details are listed here.
DrugMay 11, 2022
Losartan Potassium & Hydrochlorothiazide Tablets, USP, 100 mg/12.5 mg, a) 30-count bottles recall — FDA D-0837-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugMay 11, 2022
Losartan Potassium and Hydrochlorothiazide Tablets USP, 50 mg/12.5 mg a) 30-count bottles recall — FDA D-0841-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugMay 11, 2022
Losartan Potassium Tablets USP, 25 mg, a) 90-count bottles (NDC# 68180-376-03), b) recall — FDA D-0838-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugMay 11, 2022
McKesson Corporation dba McKesson Drug Company Betamethasone Dipropionate Ointment USP recall — FDA D-0850-2022
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Class IIFDA: OngoingMcKesson Corporation dba McKesson Drug Company
DrugMay 11, 2022
Losartan Potassium and Hydrochlorothiazide Tablets USP, 100 mg/25 mg a) 30-count bottles recall — FDA D-0842-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugMay 11, 2022
McKesson Corporation dba McKesson Drug Company Lidocaine Prilocaine Cream USP, 2.5%/2.5% Net recall — FDA D-0849-2022
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Class IIFDA: OngoingMcKesson Corporation dba McKesson Drug Company
DrugMay 11, 2022
McKesson Corporation dba McKesson Drug Company Halobetasol Propionate Ointment 0.05% Net recall — FDA D-0847-2022
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Class IIFDA: OngoingMcKesson Corporation dba McKesson Drug Company
DrugMay 11, 2022
Losartan Potassium & Hydrochlorothiazide Tablets, USP, 100 mg/25 mg, a) 30-count bottles recall — FDA D-0836-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugMay 11, 2022
Losartan Potassium and Hydrochlorothiazide Tablets USP, 100 mg/12.5 mg a) 30-count bottles recall — FDA D-0843-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugMay 11, 2022
Losartan Potassium & Hydrochlorothiazide Tablets, USP, 50 mg/12.5 mg, a) 30-count bottles recall — FDA D-0835-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugMay 11, 2022
Losartan Potassium Tablets USP, 50 mg, a) 90-count bottles (NDC# 68180-377-03), b) recall — FDA D-0839-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugMay 11, 2022
Losartan Potassium Tablets, USP, 100 mg, a) 30-count bottles (NDC # 33342-046-07), b) recall — FDA D-0834-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugMay 11, 2022
McKesson Corporation dba McKesson Drug Company Erythromycin Topical Gel USP, 2%, Net Wt 60 g recall — FDA D-0851-2022
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Class IIFDA: OngoingMcKesson Corporation dba McKesson Drug Company
DrugMay 11, 2022
McKesson Corporation dba McKesson Drug Company Lidocaine Hydrochloride Topical Solution USP recall — FDA D-0848-2022
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Class IIFDA: OngoingMcKesson Corporation dba McKesson Drug Company
DrugMay 11, 2022
Losartan Potassium Tablets USP, 100 mg, a) 90-count bottles (NDC# 68180-378-03), b) recall — FDA D-0840-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugMay 11, 2022
Losartan Potassium Tablets, USP, 25 mg, a) 90-count bottles (NDC # 33342-044-10), b) recall — FDA D-0832-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
DrugMay 11, 2022
Losartan Potassium Tablets, USP, 50 mg, a) 30-count bottles (NDC # 33342-045-07), b) recall — FDA D-0833-2022
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Class IIFDA: TerminatedMacleods Pharma Usa Inc.
VehicleMay 9, 2022
Tesla automatic emergency braking recall — NHTSA campaign 22V317000
Tesla, Inc. (Tesla) is recalling certain 2020-2021 Model 3 and 2021 Model Y vehicles. The fisheye and narrow camera cable terminals were incorrectly installed in the cable harness…
automatic emergency brakingTesla, Inc.
VehicleMay 6, 2022
Gulf States Toyota labels recall — NHTSA campaign 22V310000
Gulf States Toyota, Inc. (GST) is recalling certain 2022 4Runner, Tacoma, Highlander, and Highlander Hybrid vehicles. The load carrying capacity modification labels may not be permanent and…
labelsGulf States Toyota, Inc.
VehicleMay 5, 2022
Kia Motors column recall — NHTSA campaign 22V304000
Kia Motors America (Kia) is recalling certain 2021-2022 Rio and Forte vehicles. A bolt in the steering column may not be secured properly, which can cause the steering column to detach from…
columnKia Motors America
Medical DeviceMay 4, 2022
Siemens Medical Solutions USA syngo.via RT Image Suite upgraded to VB60 running on SOMATOM recall — FDA Z-0997-2022
Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset coordinates being displayed in the…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceMay 4, 2022
NeuMoDx Cartridge-For in vitro diagnostic use with NeuMoOx Molecular Systems with either of recall — FDA Z-1000-2022
Potential for false positive results for SARS-CoV-2 in identified lots of cartridges, when used in conjunction with assays containing SARS-CoV-2 targets (NeuMoDx" SARS-CoV-2 Test Strip Cat…
Class IIFDA: OngoingNeuMoDx Molecular Inc.
Medical DeviceMay 4, 2022
ROi CPS Convenience kits containing regard IV Start Kits: (1) regard Clinical Packaging recall — FDA Z-1004-2022
A drug kit component was recalled by its manufacturer due to the potential for inadequacy of the validation of test methods used in its manufacture.
Class IIFDA: TerminatedROi CPS LLC
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Recent recall archives
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October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories